# FDA Inspection 1034999 - Alpha Tekniko - December 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/alpha-tekniko/9577b29b-6da5-424b-85fb-b3ec8210a765
Source feed: FDA_Inspections

> FDA Inspection 1034999 for Alpha Tekniko on December 14, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034999
- Company Name: Alpha Tekniko
- Inspection Date: 2017-12-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/alpha-tekniko/8f9d6c46-17c5-4666-b797-0ebba19eb86b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7